نتائج البحث - "Srinivasan, Abhay S."

1

دورية أكاديمية

O-3 | Identification and Percutaneous Embolization of Abnormal Hepatopulmonary Lymphatic Connections

المؤلفون: Gupta, Mudit, Tomasulo, Catherine E., Ford, Brooke, Srinivasan, Abhay S., Krishnamurthy, Ganesh, Escobar, Fernando, Dori, Yoav, Smith, Christopher L.

المصدر: Journal of the Society for Cardiovascular Angiography & Interventions ; volume 2, issue 3, page 100662 ; ISSN 2772-9303

الإتاحة: https://doi.org/10.1016/j.jscai.2023.100662Test
https://api.elsevier.com/content/article/PII:S2772930323000972?httpAccept=text/xmlTest
https://api.elsevier.com/content/article/PII:S2772930323000972?httpAccept=text/plainTest

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2

دورية أكاديمية

Microcystic lymphatic malformations in Turner syndrome are due to somatic mosaicism of PIK3CA.

المؤلفون: Nriagu, Bede N., Williams, Lydia S., Brewer, Niambi, Surrey, Lea F., Srinivasan, Abhay S., Li, Dong, Britt, Allison, Treat, James, Crowley, T. Blaine, O'Connor, Nora, Ganguly, Arupa, Low, David, Queenan, Maria, Drivas, Theodore G., Zackai, Elaine H., Adams, Denise M., Hakonarson, Hakon, Snyder, Kristen M., Sheppard, Sarah E.

المصدر: American Journal of Medical Genetics. Part A; Jan2024, Vol. 194 Issue 1, p64-69, 6p

3

دورية أكاديمية

Direct Nidal Ethyl Vinyl Alcohol Copolymer Embolization With Flow Reduction Techniques as a Primary Treatment for Intraosseous Mandibular Arteriolovenous Malformations ; Report of 2 Cases

المؤلفون: Worede, Fikadu, Granquist, Eric J., Srinivasan, Abhay S., Vatsky, Seth E., Cahill, Anne Marie

المصدر: Journal of Vascular Anomalies ; volume 2, issue 3, page e021 ; ISSN 2690-2702

الإتاحة: https://doi.org/10.1097/jova.0000000000000021Test

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4

كتاب

Radiologic Evaluation of Pediatric Inflammatory Bowel Disease

المؤلفون: Acord, Michael R., Dennis, Rebecca A., Srinivasan, Abhay S., Anupindi, Sudha A.

المصدر: Pediatric Inflammatory Bowel Disease ; page 255-266 ; ISBN 9783031147432 9783031147449

الإتاحة: https://doi.org/10.1007/978-3-031-14744-9_20Test

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5

دورية أكاديمية

Pathogenic variants in PIK3CA are associated with clinical phenotypes of kaposiform lymphangiomatosis, generalized lymphatic anomaly, and central conducting lymphatic anomaly.

المؤلفون: Grenier, Jeremy M., Borst, Alexandra J., Sheppard, Sarah E., Snyder, Kristen M., Li, Dong, Surrey, Lea F., Al‐Ibraheemi, Alyaa, Weber, David R., Treat, James R., Smith, Christopher L., Laje, Pablo, Dori, Yoav, Adams, Denise M., Acord, Michael, Srinivasan, Abhay S.

المصدر: Pediatric Blood & Cancer; Sep2023, Vol. 70 Issue 9, p1-6, 6p

6

دورية أكاديمية

Microcystic lymphatic malformations in Turner syndrome are due to somatic mosaicism of PIK3CA

المؤلفون: Nriagu, Bede N., Williams, Lydia S., Brewer, Niambi, Surrey, Lea F., Srinivasan, Abhay S., Li, Dong, Britt, Allison, Treat, James, Crowley, T. Blaine, O'Connor, Nora, Ganguly, Arupa, Low, David, Queenan, Maria, Drivas, Theodore G., Zackai, Elaine H., Adams, Denise M., Hakonarson, Hakon, Snyder, Kristen M., Sheppard, Sarah E.

المساهمون: Children's Hospital of Philadelphia, Eunice Kennedy Shriver National Institute of Child Health and Human Development

المصدر: American Journal of Medical Genetics Part A ; volume 194, issue 1, page 64-69 ; ISSN 1552-4825 1552-4833

الإتاحة: https://doi.org/10.1002/ajmg.a.63385Test

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7

دورية أكاديمية

Pathogenic variants in PIK3CAare associated with clinical phenotypes of kaposiform lymphangiomatosis, generalized lymphatic anomaly, and central conducting lymphatic anomaly

المؤلفون: Grenier, Jeremy M., Borst, Alexandra J., Sheppard, Sarah E., Snyder, Kristen M., Li, Dong, Surrey, Lea F., Al‐Ibraheemi, Alyaa, Weber, David R., Treat, James R., Smith, Christopher L., Laje, Pablo, Dori, Yoav, Adams, Denise M., Acord, Michael, Srinivasan, Abhay S.

المساهمون: Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health

المصدر: Pediatric Blood & Cancer ; volume 70, issue 9 ; ISSN 1545-5009 1545-5017

الإتاحة: https://doi.org/10.1002/pbc.30419Test

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8

دورية أكاديمية

Genomic profiling informs diagnoses and treatment in vascular anomalies

المؤلفون: Li, Dong, Sheppard, Sarah E., March, Michael E., Battig, Mark R., Surrey, Lea F., Srinivasan, Abhay S., Matsuoka, Leticia S., Tian, Lifeng, Wang, Fengxiang, Seiler, Christoph, Dayneka, Jill, Borst, Alexandra J., Matos, Mary C., Paulissen, Scott M., Krishnamurthy, Ganesh, Nriagu, Bede, Sikder, Tamjeed, Casey, Melissa, Williams, Lydia, Rangu, Sneha, O’Connor, Nora, Thomas, Alexandria, Pinto, Erin, Hou, Cuiping, Nguyen, Kenny, Pellegrino da Silva, Renata, Chehimi, Samar N., Kao, Charlly, Biroc, Lauren, Britt, Allison D., Queenan, Maria, Reid, Janet R., Napoli, Joseph A., Low, David M., Vatsky, Seth, Treat, James, Smith, Christopher L., Cahill, Anne Marie, Snyder, Kristen M., Adams, Denise M., Dori, Yoav, Hakonarson, Hakon

المساهمون: U.S. Department of Health & Human Services | NIH | National Center for Advancing Translational Sciences, U.S. Department of Health & Human Services | NIH | Eunice Kennedy Shriver National Institute of Child Health and Human Development

المصدر: Nature Medicine ; volume 29, issue 6, page 1530-1539 ; ISSN 1078-8956 1546-170X

مصطلحات موضوعية: General Biochemistry, Genetics and Molecular Biology, General Medicine

الإتاحة: https://doi.org/10.1038/s41591-023-02364-xTest
https://www.nature.com/articles/s41591-023-02364-x.pdfTest
https://www.nature.com/articles/s41591-023-02364-xTest

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